Synthesis of azecino[5,4-b]indoles and indolo[3,2-e][2]benzazonines via tandem transformation of hydrogenated indoloquinolizines and indolizines

The reactions of partially hydrogenated indole-fused quinolizines and indolizines with activated alkynes in methanol, acetonitrile, and dichloromethane were studied. The reactions were shown to be accompanied by the cleavage of the bridging C-N bond. Azecino[5,4-b]-indole and indolo[3,2-e][2]benzazonine derivatives were synthesized. © 2012 Springer Science+Business Media New York.

Авторы
Номер выпуска
6
Язык
Английский
Страницы
1231-1241
Статус
Опубликовано
Том
61
Год
2012
Организации
  • 1 Peoples' Friendship University of Russia, 6 ul. Miklukho-Maklaya, 117198 Moscow, Russian Federation
  • 2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991 Moscow, Russian Federation
  • 3 N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 31 Leninsky prosp, 119991 Moscow, Russian Federation
Ключевые слова
alkynes; azecino[5,4-b]indoles; domino reactions; eburnamenine; hydrogenated indolizines and quinolizines; indolo[3,2-e][2]benzazonines
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/2308/
Поделиться

Другие записи